Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/A/T|Ancestral: C|Ambiguity code: H
Location

Chromosome 4:154585711 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Splice acceptor variant
Evidence status

Clinical significance

Synonyms

LSDB 1934

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant overlaps 10 transcripts and is associated with 2 phenotypes.

Variant displays